From your product data to a filing-ready verdict.
There is nothing to configure. A submission enters one of two ways, is normalised into a substance list, screened against 13 EU lists, verdicted, reported and logged, with a person in the loop for the highest-risk results.
From Safety Data Sheet to filing-ready verdict: six stages, minutes end to end.
Watch a submission travel the pipeline. Each stage applies a specific compliance rule: extraction integrity, list matching, concentration limits, Annex XVII conditions, and an engineer review before anything high-risk is released.
Intake
- In
- SDS PDF or declared list
- Out
- One normalised submission
Upload a Safety Data Sheet, or declare substances by name, CAS, EC and concentration. Multi-part documents are accepted.
Extract
- In
- Composition tables
- Out
- Structured substance rows
Every composition table is read across all parts of the document and returned as rows with name, CAS, EC and concentration.
Screen
- In
- Substance rows
- Out
- Matches per list
Each substance is matched by CAS against the 13 EU lists: REACH SVHC, Annex XIV, Annex XVII, RoHS, POPs, PFAS, Battery and the rest.
Evaluate
- In
- Matches and concentrations
- Out
- Per-substance findings
Concentration thresholds, group sum-rules for phthalates and PFAS, Annex XVII conditions by article category, and applicable exemptions.
Verdict
- In
- Per-substance findings
- Out
- RED, AMBER or GREEN
Findings aggregate to one product verdict with Article 33 text, phase-out dates, safer alternatives and a CSV of every substance.
Release
- In
- Verdict and report
- Out
- Delivered and logged
RED holds for review by a compliance engineer. AMBER and GREEN are released automatically to email and the portal.
Four outcomes, always paired with the word.
Colour is never the only signal. Every verdict carries its label, its reason and the list entry it rests on.
No listed substance at or above its threshold. Nothing to declare; keep the report for your records and re-screen on the next update.
A duty applies but the product can stay on the market: typically an SVHC at ≥ 0.1 % (Article 33 communication) or a substance near a limit. Actions are listed.
A restricted or authorisation-only substance is over its limit (Annex XVII, Annex XIV, RoHS, POPs). Held for expert review before release, with substitution options.
The data cannot support a verdict: a missing concentration, a scanned PDF, an incomplete extraction. Verachek stops and tells you what is needed rather than guessing.
Anatomy of a Verachek report.
| Section | What it tells you |
|---|---|
| Verdict & callout | Overall RED / AMBER / GREEN with the one-line reason and the next action. |
| Composition & identification | Every substance with name, CAS, EC and concentration exactly as received, N/A where the source omits data. |
| Regulatory screening results | Per list: the entry matched, the limit, and whether the concentration is over or within it. Sum-rules and derogations shown where applied. |
| Article 33 declaration | Auto-generated when an SVHC is present at ≥ 0.1 % w/w, ready to pass down the supply chain. |
| Hits by list | The bar chart you see in the demo: how many substances hit each list. |
| Exposure & enforcement | Occupational exposure limits and real-world enforcement cross-references for the substances found. |
| Derogations & phase-out timeline | Category exemptions that apply, and dated authorisation / sunset dates so you can plan substitution. |
| Safer alternatives | Curated substitution options per flagged substance, with regrettable-substitution checks. |
| Data-quality notes | Extraction completeness, CAS mismatches, missing values, so you know how much to trust the result. |
| Exports | Shareable link, PDF, and a clean CSV of every substance and its status. |
This article contains formaldehyde (CAS 84-61-7, EC 201-545-9), a substance on the REACH Candidate List of Substances of Very High Concern, at a concentration above 0.1 % w/w.
Sufficient information to allow safe use: avoid skin contact with the uncured product; wear protective gloves; refer to the Safety Data Sheet, sections 7 and 8.
Knowledge base: Candidate List as of 4 February 2026 (253 entries). Verachek · automated regulatory screening · does not constitute legal advice.
The Article 33 text is a starting point. Under REACH the duty-holder must supply the recipient with sufficient information to allow safe use, adapt the safe-use line to your product.
The guards that make the verdict worth filing.
Truthful identifiers
Substances are reported exactly as received. A missing identifier is shown as missing, never invented or borrowed.
Conservative on concentrations
Concentrations are read in the formats suppliers actually use and assessed conservatively. A blank value is flagged, never assumed to be zero.
No false GREEN
If a document cannot be read completely and reliably, the result is a FLAG with the reason, never a clean verdict.
Engineer review on RED
Every RED verdict is approved or corrected by a compliance engineer before release. Professional and Business plans get priority turnaround.